Canonical Allele Identifier: CA495566631
Gene: SLC6A2 HGNC NCBI

Linked Data

dbSNP Id: rs1323355662

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55696265T>A , CM000678.2:g.55696265T>A GRCh38
NC_000016.9:g.55730177T>A , CM000678.1:g.55730177T>A GRCh37
NC_000016.8:g.54287678T>A NCBI36
NG_016969.1:g.45636T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219833.13:c.1188T>A ENSP00000219833.8:p.Ser396=
ENST00000568943.6:c.1188T>A MANE Select ENSP00000457473.1:p.Ser396=
ENST00000574918.2:c.1053T>A ENSP00000460214.2:p.Ser351=
ENST00000682050.1:c.1012+863T>A ENSP00000508367.1:n.1012+863T>A
ENST00000219833.12:c.1188T>A ENSP00000219833.8:p.Ser396=
ENST00000379906.6:c.1188T>A ENSP00000369237.2:p.Ser396=
ENST00000414754.7:c.1188T>A ENSP00000394956.3:p.Ser396=
ENST00000561820.5:c.1188T>A ENSP00000454439.1:p.Ser396=
ENST00000566163.5:c.1053T>A ENSP00000456210.1:p.Ser351=
ENST00000567238.1:c.873T>A ENSP00000457375.1:p.Ser291=
ENST00000568943.5:c.1188T>A ENSP00000457473.1:p.Ser396=
NM_001043.3:c.1188T>A NP_001034.1:p.Ser396=
NM_001172501.1:c.1188T>A NP_001165972.1:p.Ser396=
NM_001172502.1:c.873T>A NP_001165973.1:p.Ser291=
NM_001172504.1:c.1188T>A NP_001165975.1:p.Ser396=
XM_006721263.2:c.1188T>A XP_006721326.1:p.Ser396=
XM_011523295.1:c.1188T>A XP_011521597.1:p.Ser396=
XM_011523296.1:c.1053T>A XP_011521598.1:p.Ser351=
XM_011523297.1:c.1053T>A XP_011521599.1:p.Ser351=
XM_011523298.1:c.1147+863T>A XP_011521600.1:n.1147+863T>A
XM_011523299.1:c.465T>A XP_011521601.1:p.Ser155=
XM_011523300.1:c.465T>A XP_011521602.1:p.Ser155=
XR_933403.1:n.1805T>A
XM_011523295.2:c.1188T>A XP_011521597.1:p.Ser396=
XM_011523296.2:c.1053T>A XP_011521598.1:p.Ser351=
XM_011523297.3:c.1053T>A XP_011521599.1:p.Ser351=
XM_011523298.2:c.1147+863T>A XP_011521600.1:n.1147+863T>A
XM_011523299.2:c.465T>A XP_011521601.1:p.Ser155=
XM_011523300.2:c.465T>A XP_011521602.1:p.Ser155=
XR_933403.3:n.1481T>A
NM_001172501.2:c.1188T>A NP_001165972.1:p.Ser396=
NM_001172501.3:c.1188T>A MANE Select NP_001165972.1:p.Ser396=